(Q30871448)

27 June 2017

title

Overexpressed protein disulfide isomerase in brains of patients with sporadic Creutzfeldt-Jakob disease (English)

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sporadic Creutzfeldt-Jakob disease

27 June 2017

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Gert Lubec

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ORCID Public Data File 2021

author name string

Byong Chul Yoo

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27 June 2017

Kurt Krapfenbauer

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27 June 2017

Nigel Cairns

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27 June 2017

Girma Belay

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27 June 2017

Michal Bajo

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27 June 2017

language of work or name

English

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publication date

1 December 2002

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27 June 2017

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27 June 2017

volume

334

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27 June 2017

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27 June 2017

page(s)

196-200

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The spatial patterns of prion protein deposits in Creutzfeldt-Jakob disease: comparison with beta-amyloid deposits in Alzheimer's disease

27 June 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Prion protein glycosylation is sensitive to redox change

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Binding of disease-associated prion protein to plasminogen.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Identification of Proteins by Matrix-Assisted Laser Desorption Ionization–Mass Spectrometry Following In-Gel Digestion in Low-Salt, Nonvolatile Buffer and Simplified Peptide Recovery

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Protein disulfide-isomerase

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Effect of protein application mode and acrylamide concentration on the resolution of protein spots separated by two‐dimensional gel electrophoresis

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

High-level expression and characterization of a purified 142-residue polypeptide of the prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

1 reference

7 January 2021

Thioredoxin converts the Syrian hamster (29-231) recombinant prion protein to an insoluble form

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Drebrin, a dendritic spine protein, is manifold decreased in brains of patients with Alzheimer's disease and Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

A role for intermolecular disulfide bonds in prion diseases?

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Neurobiology: p25 protein in neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

Physical studies of conformational plasticity in a recombinant prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901071-6

7 January 2021

10.1016/S0304-3940(02)01071-6

Identifiers

DOI

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27 June 2017

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